Home NDC 85828-301 GO HOME AND HAVEN ANTIBACTERIAL HAND WIPES
Product NDC 85828-301
11-digit product format 858280301
Labeler code 85828
Product ID 85828-301_4a5ffc48-abde-c7bb-e063-6394a90afe3a
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride
Dosage form CLOTH
Route TOPICAL
Labeler Grocery Outlet Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-01
Substance BENZALKONIUM CHLORIDE
Active strength .13 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base GO HOME AND HAVEN ANTIBACTERIAL HAND WIPES
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038558 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85828-301-01 85828030101 124 g in 1 POUCH (85828-301-01) 124 g 2026-06-01 No No Current